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Gemcitabine

Generic Name
Gemcitabine
Brand Names
Gemzar
Drug Type
Small Molecule
Chemical Formula
C9H11F2N3O4
CAS Number
95058-81-4
Unique Ingredient Identifier
B76N6SBZ8R
Background

Gemcitabine is a nucleoside analog and a chemotherapeutic agent. It was originally investigated for its antiviral effects, but it is now used as an anticancer therapy for various cancers. Gemcitabine is a cytidine analog with two fluorine atoms replacing the hydroxyl on the ribose. As a prodrug, gemcitabine is transformed into its active metabolites that work by replacing the building blocks of nucleic acids during DNA elongation, arresting tumour growth and promoting apoptosis of malignant cells. The structure, metabolism, and mechanism of action of gemcitabine are similar to cytarabine, but gemcitabine has a wider spectrum of antitumour activity.

Gemcitabine is marketed as Gemzar and it is available as intravenous injection. It is approved by the FDA to treat advanced ovarian cancer in combination with carboplatin, metastatic breast cancer in combination with paclitaxel, non-small cell lung cancer in combination with cisplatin, and pancreatic cancer as monotherapy. It is also being investigated in other cancer and tumour types.

Indication

Gemcitabine is a chemotherapeutic agent used as monotherapy or in combination with other anticancer agents.

In combination with carboplatin, it is indicated for the treatment of advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy.

Gemcitabine in combination with paclitaxel is indicated for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated.

In combination with cisplatin, gemcitabine is indicated for the first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer (NSCLC). Dual therapy with cisplatin is also used to treat patients with Stage IV (locally advanced or metastatic) transitional cell carcinoma (TCC) of the bladder.

Gemcitabine is indicated as first-line treatment for patients with locally advanced (nonresectable Stage II or Stage III) or metastatic (Stage IV) adenocarcinoma of the pancreas. Gemcitabine is indicated for patients previously treated with fluorouracil.

Associated Conditions
Advanced Ovarian Cancer, Bladder Transitional Cell Carcinoma Stage IV, Carcinoma of the Head and Neck, Cervical Cancer, Cutaneous T-Cell Lymphoma (CTCL), Hodgkins Disease (HD), Mesothelioma, Metastatic Breast Cancer, Pancreatic Adenocarcinoma Locally Advanced, Small Cell Lung Cancer (SCLC), Stage IIIA Non Small Cell Lung Cancer, Stage IIIB Non-Small Cell Lung Cancer, Stage IV Non-small Cell Lung Cancer (NSCLC), Stage 4 Pancreatic adenocarcinoma
Associated Therapies
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Study of Robatumumab (SCH 717454, MK-7454) in Combination With Different Treatment Regimens in Participants With Advanced Solid Tumors (P04722, MK-7454-004)

Phase 1
Terminated
Conditions
Neoplasms
Interventions
First Posted Date
2009-08-07
Last Posted Date
2018-08-24
Lead Sponsor
Merck Sharp & Dohme LLC
Target Recruit Count
15
Registration Number
NCT00954512

A Study of Tarceva (Erlotinib) in Sequential Combination With Gemcitabine as First Line Therapy in Patients With Advanced Non-Small Cell Lung Cancer

Phase 2
Terminated
Conditions
Non-Small Cell Lung Cancer
Interventions
First Posted Date
2009-07-16
Last Posted Date
2015-04-02
Lead Sponsor
Hoffmann-La Roche
Target Recruit Count
54
Registration Number
NCT00940875

Cediranib Versus Placebo Plus Cisplatin/Gemcitabine Chemotherapy for Patients With Advanced Biliary Tract Cancers

Phase 2
Completed
Conditions
Biliary Tract Neoplasms
Interventions
First Posted Date
2009-07-15
Last Posted Date
2014-10-27
Lead Sponsor
University College, London
Target Recruit Count
124
Registration Number
NCT00939848
Locations
🇬🇧

University College London Hospitals NHS Foundation Trust, London, United Kingdom

🇬🇧

The Christie NHS Foundation Trust, Manchester, United Kingdom

Safety and Tolerability Study of AZD7762 in Combination With Gemcitabine

Phase 1
Terminated
Conditions
Cancer
Solid Tumors
Advanced Solid Malignancies
Interventions
Drug: AZD7762
Drug: gemcitabine
First Posted Date
2009-07-13
Last Posted Date
2011-02-07
Lead Sponsor
AstraZeneca
Target Recruit Count
24
Registration Number
NCT00937664
Locations
🇯🇵

Research Site, Minami-ku, Fukuoka, Japan

High-dose Chemotherapy for Poor-Prognosis Relapsed Germ-Cell Tumors

Phase 2
Completed
Conditions
Testicular Cancer
Interventions
First Posted Date
2009-07-10
Last Posted Date
2024-08-26
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
64
Registration Number
NCT00936936
Locations
🇺🇸

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

🇺🇸

Fred Hutchinson Cancer Center, Seattle, Washington, United States

A Phase II Study of Neo-Adjuvant Gemcitabine, Cisplatin and Bevacizumab in Stage IIIA (N2) Non-Squamous Cell Non-Small Cell Lung Cancer

Phase 2
Terminated
Conditions
NSCLC
Stage IIIA (N2)
Interventions
First Posted Date
2009-06-18
Last Posted Date
2018-11-30
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
7
Registration Number
NCT00924209
Locations
🇺🇸

National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States

🇭🇷

University Hospital for Lung Diseases, Zagreb, Croatia

Gemcitabine and Cisplatin Plus Sorafenib in Patients With Advanced Biliary Tract Carcinomas Naive to Systemic Therapy

Phase 2
Completed
Conditions
Extrahepatic Bile Duct Cancer
Gallbladder Cancer
Interventions
First Posted Date
2009-06-12
Last Posted Date
2016-02-03
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Target Recruit Count
39
Registration Number
NCT00919061
Locations
🇺🇸

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Vorinostat, Carboplatin and Gemcitabine in Women With Recurrent, Platinum-Sensitive Ovarian Cancer

Phase 1
Terminated
Conditions
Ovarian Cancer
Fallopian Tube Cancer
Peritoneal Cancer
Interventions
First Posted Date
2009-05-29
Last Posted Date
2018-09-10
Lead Sponsor
Dana-Farber Cancer Institute
Target Recruit Count
15
Registration Number
NCT00910000
Locations
🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

🇺🇸

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

A Phase I/II Open-Label Dose-Escalation Clinical Trial of CPI-613 in Combination With Gemcitabine in Cancer Patients

Phase 1
Terminated
Conditions
Pancreatic Cancer
Cancer
Pancreatic Carcinoma
Interventions
Drug: CPI-613
Drug: Gemcitabine
First Posted Date
2009-05-22
Last Posted Date
2017-03-21
Lead Sponsor
Cornerstone Pharmaceuticals
Target Recruit Count
6
Registration Number
NCT00907166
Locations
🇺🇸

Eastchester Center for Cancer Care, Bronx, New York, United States

🇺🇸

Mary Crowley Cancer Research Centers, Dallas, Texas, United States

Study Of The Effect Of CP-751,871 In Combination With Gemcitabine And Cisplatin In Patients With Advanced Non-Small Cell Lung Cancer

Phase 3
Withdrawn
Conditions
Carcinoma, Non-Small-Cell Lung
Interventions
First Posted Date
2009-05-22
Last Posted Date
2014-06-17
Lead Sponsor
Pfizer
Registration Number
NCT00907504
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